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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
1999 1
2000 1
2002 2
2003 1
2004 4
2005 1
2006 4
2007 2
2009 2
2010 5
2011 8
2012 15
2013 8
2014 6
2015 9
2016 7
2017 10
2018 15
2019 14
2020 20
2021 21
2022 24
2023 15
2024 4
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167 results

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Page 1
Glycogen storage diseases: An update.
Gümüş E, Özen H. Gümüş E, et al. World J Gastroenterol. 2023 Jul 7;29(25):3932-3963. doi: 10.3748/wjg.v29.i25.3932. World J Gastroenterol. 2023. PMID: 37476587 Free PMC article. Review.
Apolipoprotein E allelic variants and cerebral palsy.
Gümüş E, Aras BD, Çilingir O, Yarar C, Çarman KB, Laçiner-Gürlevik S, Koçak O, Artan S. Gümüş E, et al. Turk J Pediatr. 2018;60(4):361-371. doi: 10.24953/turkjped.2018.04.002. Turk J Pediatr. 2018. PMID: 30859759 Free article.
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome.
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Caldas Rosa ECC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban-Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Lima AR, et al. Among authors: gumus e. Hum Mutat. 2022 Jul;43(7):900-918. doi: 10.1002/humu.24375. Epub 2022 May 10. Hum Mutat. 2022. PMID: 35344616 Free PMC article.
Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.
Himmelreich N, Bertoldi M, Alfadhel M, Alghamdi MA, Anikster Y, Bao X, Bashiri FA, Zeev BB, Bisello G, Ceylan AC, Chien YH, Choy YS, Elsea SH, Flint L, García-Cazorla À, Gijavanekar C, Gümüş EY, Hamad MH, Hişmi B, Honzik T, Hübschmann OK, Hwu WL, Ibáñez-Micó S, Jeltsch K, Juliá-Palacios N, Kasapkara ÇS, Kurian MA, Kusmierska K, Liu N, Ngu LH, Odom JD, Ong WP, Opladen T, Oppeboen M, Pearl PL, Pérez B, Pons R, Rygiel AM, Shien TE, Spaull R, Sykut-Cegielska J, Tabarki B, Tangeraas T, Thöny B, Wassenberg T, Wen Y, Yakob Y, Yin JGC, Zeman J, Blau N. Himmelreich N, et al. Among authors: gumus ey. Mol Genet Metab. 2023 Jul;139(3):107624. doi: 10.1016/j.ymgme.2023.107624. Epub 2023 Jun 2. Mol Genet Metab. 2023. PMID: 37348148 Free article.
An unusual cause of diarrhea in a child with nephrotic syndrome: Answers.
Baltu D, Kurt Sukur ED, Gumus E, Tastemel Ozturk T, Ergen YM, Demirtas D, Gülhan B, Ozaltin F, Orhan D, Özen H, Düzova A. Baltu D, et al. Among authors: gumus e. Pediatr Nephrol. 2023 Dec;38(12):3977-3981. doi: 10.1007/s00467-023-06021-w. Epub 2023 May 24. Pediatr Nephrol. 2023. PMID: 37222936 No abstract available.
An unusual cause of diarrhea in a child with nephrotic syndrome: Questions.
Baltu D, Kurt Sukur ED, Gumus E, Tastemel Ozturk T, Ergen YM, Demirtas D, Gülhan B, Ozaltin F, Orhan D, Özen H, Düzova A. Baltu D, et al. Among authors: gumus e. Pediatr Nephrol. 2023 Dec;38(12):3975-3976. doi: 10.1007/s00467-023-06020-x. Epub 2023 May 24. Pediatr Nephrol. 2023. PMID: 37222935 No abstract available.
167 results